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Master's Dissertation
DOI
https://doi.org/10.11606/D.5.2005.tde-19102005-105311
Document
Author
Full name
Marcia Perez Resende Oliveros
Institute/School/College
Knowledge Area
Date of Defense
Published
São Paulo, 2005
Supervisor
Committee
Lopez, Luis Fernandez (President)
Diaz, Ricardo Sobhie
Durigon, Edison Luiz
Title in Portuguese
"Prevalência e covariação de mutações relacionadas à resistência aos inibidores de protease no subtipo F do HIV-1"
Keywords in Portuguese
BASES DE DADOS
INIBIDORES DE PROTEASE HIV
MUTAÇÃO
POLIMORFISMO (GENÉTICA)
PREVALÊNCIA
Abstract in Portuguese
Cada subtipo de HIV-1 tem um padrão mutacional próprio. Dados sobre mutações de resistência aos antiretrovirais foram obtidos com o subtipo B, primeiro em prevalência no Brasil. O segundo em algumas regiões é o subtipo F. Foram analisados padrões mutacionais em seqüências brasileiras de protease do subtipo F e levantou as seqüências deste subtipo disponíveis na base de dados de Stanford. A análise de dois grupos de seqüências (pacientes não tratados e tratados com inibidores de protease) mostrou 19 mutações associadas ao tratamento comuns ao subtipo B e 17 duplas de mutações associadas ao tratamento que diferem das descritas para o subtipo B, indicando a necessidade de estudos sobre rotas mutacionais no subtipo F.
Title in English
Prevalence and covariation of protease inhibitor resistance related mutations of HIV type 1 subtype F
Keywords in English
DATABASES
MUTATION
POLYMORFISM (GENETICS)
PREVALENCE
PROTEASE INHIBITORS
Abstract in English
Each HIV-1 subtype has a specific mutation pattern. Data on HIV-1 antiretroviral resistance mutations were obtained with subtype B, the first in prevalence in Brazil. The second in some regions is subtype F. Mutation patterns of Brazilian subtype F protease sequences were analyzed and performed a research of the sequences of Stanford Database. The analysis of two groups of sequences (untreated and treated patients with protease inhibitors) showed 19 treatment associated mutations also common in subtype B and 17 combinations of statistically treatment associated mutations that were quite different to those described for subtype B, indicating the need of studies to evaluate specific mutation pathways of subtype F.
 
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Publishing Date
2005-10-20
 
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